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Deeping in the Role of the MAP-Kinases Interacting Kinases (MNKs) in Cancer
- Source :
- International Journal of Molecular Sciences, International Journal of Molecular Sciences, Vol 21, Iss 2967, p 2967 (2020)
- Publication Year :
- 2020
-
Abstract
- The mitogen-activated protein kinase (MAPK)-interacting kinases (MNKs) are involved in oncogenic transformation and can promote metastasis and tumor progression. In human cells, there are four MNKs isoforms (MNK1a/b and MNK2a/b), derived from two genes by alternative splicing. These kinases play an important role controlling the expression of specific proteins involved in cell cycle, cell survival and cell motility via eukaryotic initiation factor 4E (eIF4E) regulation, but also through other substrates such as heterogeneous nuclear ribonucleoprotein A1, polypyrimidine tract-binding protein-associated splicing factor and Sprouty 2. In this review, we provide an overview of the role of MNK in human cancers, describing the studies conducted to date to elucidate the mechanism involved in the action of MNKs, as well as the development of MNK inhibitors in different hematological cancers and solid tumors.
- Subjects :
- MAPK/ERK pathway
Cell Survival
MNK
Antineoplastic Agents
Review
Biology
Protein Serine-Threonine Kinases
Catalysis
lcsh:Chemistry
Inorganic Chemistry
Splicing factor
Cell Line, Tumor
Neoplasms
Animals
Humans
cancer
metastasis
Physical and Theoretical Chemistry
Protein kinase A
lcsh:QH301-705.5
Molecular Biology
Protein Kinase Inhibitors
Spectroscopy
therapy
Kinase
Organic Chemistry
Alternative splicing
EIF4E
Cell Cycle
Intracellular Signaling Peptides and Proteins
General Medicine
Prognosis
antitumor drug
Computer Science Applications
Cell biology
lcsh:Biology (General)
lcsh:QD1-999
Tumor progression
eIF4E
Heterogeneous Nuclear Ribonucleoprotein A1
Disease Susceptibility
Biomarkers
Subjects
Details
- ISSN :
- 14220067
- Volume :
- 21
- Issue :
- 8
- Database :
- OpenAIRE
- Journal :
- International journal of molecular sciences
- Accession number :
- edsair.doi.dedup.....e9df6bcd7888483f4a07d9ff4a57c02d